ZFIN Human Disease: Worth syndrome

OBO ID: DOID:0080037

Term Name:	Worth syndrome		Search Ontology:
Synonyms:	autosomal dominant endosteal hyperostosis autosomal dominant osteosclerosis benign form of Worth hyperostosis corticalis generalisata with torus platinus Worth's syndrome
Definition:	A hyperostosis that has_material_basis_in a mutation in the LRP5 gene which results_in increased bone density and bony structures located_in palate. (4)
References:	GARD:390 MESH:C536748 OMIM:144750 ORDO:2790 SNOMEDCT_US_2023_03_01:254131007 UMLS_CUI:C0432273
Ontology:	Human Disease ( DOID:0080037 )

Relationships

is a type of:	autosomal dominant disease hyperostosis autosomal dominant disease hyperostosis Show first 5 Terms

OTHER Worth syndrome PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
LRP5	lrp5	Endosteal hyperostosis	144750

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None